US3014888A

US3014888A - Stabilized hydrocarbon compositions

Info

Publication number: US3014888A
Application number: US779540A
Authority: US
Inventors: James D Shimmin; Vivian A Moffatt
Original assignee: Shell Oil Co
Current assignee: Shell USA Inc
Priority date: 1957-12-20
Filing date: 1958-12-11
Publication date: 1961-12-26
Anticipated expiration: 1978-12-26

Description

United States Patent Cfifice 3,014,888 Patented Dec. 26, 1961 STABILIZED HYDRUCARBQN C(EMPGSITIQNS James D. Shinrmin, Little Sutton, Wirral, and Vivian A.

Motiatt, Wirral, England, assignors to Shell Gil Company, a corporation of Delaware No Drawing. Filed Bree. 11, 195%, Ser. No. 779,540 Claims priority, application Great Britain Bee. 2%), 1957 5 Claims. (Cl. zen-45s The present invention relates to hydrocarbon compositions which are stabilized against oxidation and color changes.

Many liquid and solid hydrocarbons tend to deteriorate due to oxidation resulting in the formation of undesirable and deleterious products which render them useless for their intended purposes Within a relatively short period of time. Hydrocarbon materials subject to such deterioration include petroleum hydrocarbons having more than 5 carbon atoms and polymeric hydrocarbons prepared by the polymerization of monoolefins. These polymeric hydrocarbons, especially when prepared by the so-called low pressure process as described below, tend to degrade when there is no antioxidant present, and the addition of an antioxidant to ofiset this usually leads to undesirable color formation. The exact mechanism of this discoloration is not fully understood, but it is believed likely that in the case of the polymeric hydrocarbon materials prepared by the low pressure process, the discoloration is caused by minute traces of the catalyst remaining in the finished polymeric hydrocarbon material.

It is known that phenothiazine has antioxidant properties, and it and many of its derivatives have been suggested for use as antioxidants in synthetic lubricating oils such as di(2-ethylhexyl) sebacate, dinonyl sebacate, and dinonyl adipate.

However, phenothiazine and many of its derivatives have the disadvantage of forming a black precipitate when used in hydrocarbon oils because of instability in the presence of light. Thus, while phenothiazine has good antioxidant properties, light and catalyst such as the Ziegler type catalyst cause undesirable black coloration, and render phenothiazine unsatisfactory for many purposes. This is particularly the case with polyethylene and polypropylene where color is often the critical factor.

It has now been found, quite unexpectedly, that both oxidation stabflity and color stability of hydrocarbons can be improved by the addition of a minor proportion of a phenothiazine derivative which has benzyl or a substituted benzyl group in the l-position.

It is an object of this invention to provide hydrocarbon materials having improved stability against oxidation and color deterioration. Another object of this invention is to provide a stabilized polymerization product of olefins, particularly polyethylene and polypropylene or mixtures thereof which have good color retention and are stable against oxidation which tends to cause brittleness and other losses of desired physical properties.

These and other objects are accomplished by incorporating into a hydrocarbon composition between 0.001% and by weight of a phenothiazine having the formula R 9 1LT) 1 s 2 Where R is a member of the class consisting of a benzyl group and a substituted benzyl group.

It is critical that the group R, which is bonded to the nitrogen (in the Ill-position) be either a benzyl group or a substituted benzyl group, and the benzyl group is preferred. Substituted benzyl groups have substitutions on the aromatic portion of the benzyl group which may be alkyl groups such as methyl or ethyl groups. It is also permissible to have alkyl groups such as methyl or ethyl groups in positions 1 to 4 or 6 to 9 in the formula above. Thus it is seen, that the additive in this invention must be a IO-benzyi phenothiazine with alkyl substitutions being permissible in the aromatic portions of both the benzyl group and the phenothiazine constituents of the molecule.

The phenothiazine derivatives of the present invention are generally used in an amount between .0001% and 5% by weight based on the Weight of the whole composition. Preferably, the amounts are between 0.1% and 0.5% by weight in hydrocarbon polymers such as polyethylene and polypropylene, and between 0.2% and 2% by weight in hydrocarbon oils such as lubricating oils. The phenothiazine derivatives of this invention may be used in conjunction with any other known additive for the particular hydrocarbon composition used.

The hydrocarbons most applicable to the present invention are polymers of l-olefins having from 2 to 5 carbon atoms made by a low pressure polymerization process.

As mentioned above the phenothiazine derivatives of the present invention are particularly useful when employed in polymeric hydrocarbon substances formed from olefins such as ethylene or propylene, particularly those which have been prepared by the so-called low pressure process. A low pressure process involves the catalytic polymerization of the olefin at pressures below 500 atmospheres and the expression low pressure is thus used to distinguish the process broadly from known ethylene polymerization processes which are carried out at pressures in the neighborhood of 1,000 atmospheres or more. Examples of the catalysts which can be used in the low pressure processes as follows:

(I) The Ziegler catalyst, which term in this specification is intended to mean a catalyst formed by mixing at least one A component with at least one B component as hereinafter defined.

An A component is defined as a compound of a metal of groups 4a, 5a, 6a, 7a or 8 of the periodic classification and a B component is defined as an element or compound of the following kind:

(1) .A. group 1, 2 or 3 metal, zinc or aluminum or an alloy thereof; or

(2) An organo-metallic compound or a hydride of a group 1, 2 or,3 metal, tin or lead; or

(3) An or anic boron compound or an addition complex thereof.

In accordance with current practice the term organemetallic compound means a compound (other than an inorganic metal carbide) in which the metal is directly attached to a carbon atom. The organo-metallic compound or hydride may be in the form of a molecular compound with an ether, thioether or amine or a complex compound with an alkali metal hydride, alkali metal alkyl, alkali metal aryl or alkali metal halide. The addition complex of the organic boron compound may be a complex compound of an alkali metal hydride with a boron compound of the general formula BFRR", in which R, R" and R' represent hydrocarbon radicals, alkoxy or aryloxy groups or hydrogen atoms.

Preferably the B component of the catalyst or at least one of the B components where a plurality of B components is employed in an organo-metallic compound in which a hydrocarbon radical (preferably an alkyl radical) is attached to the metal, and in the case of those organometallic compounds which are derived from polyvalent metals the remaining valency or valencies of the metal is or are satisfied by hydrocarbon radicals, alkoxy .or

aryloxy radicals, halogen atoms or hydrogenations. Prefarably the A component of the catalyst or at least one of the A components Where a plurality of A components is employed is an inorganic halogen-containing compound of a metal of groups 4a, 5a, 6a, 7a or 8.

Particular examples of Ziegler catalysts include those formed by mixing at least one component A comprising an inorganic halide of a metal of groups 4a, 5a, 6a or 7a and particularly of groups 4a, 5a and 6a and more particularly of group 4a of the periodic table such for example as a titanium tetraand/ or tri-halide, with at least one component B comprising either:

(1) An aluminum trialkyl; or

(2) An aluminum compound of the general formula R R AlX, wherein R and R are similar or dissimilar and each represents a hydrogen atom or a hydrocarbon radical such as an alkyl, alkaryl, aryl, aralkyl, alkenyl, alkynyl, cycloalkyl, or cycloalkenyl radical and X represents a hydrogen atom, a halogen atom, an alkoxy group or an aryloxy group or the residue of a secondary amine or amide, mercaptan, thiophenol, carboxylic acid or sulphonic acid; or

(3) An aluminum compound of the general formula RA1X1X2, wherein R represents a hydrogen atom or a hydrocarbon radical as in (2) above, and X and X are similar or dissimilar and each represents a halogen atom, an alkoxy group or an aryloxy group.

Such catalysts are referred to for example in British Patent No. 799,823.

(I!) A mixture comprising aluminum trichloride, titanium tetrachloride, and aluminum powder.

(Ill) Chromoxide on a 90% silica-l0% alumina. support such as that shown in US. Patent 2,825,721. Other ratios of silica and alumina may be used, and, if desired, the catalyst may be stabilized with strontium oxide.

(IV) An oxide of a metal of the VI group of the periodic system on a support if desired in the presence of an alkali metal.

The present invention is particularly applicable to polyethylenes and polypropylenes made by using a catalyst of the Ziegler type as for example by mixing aluminum triethyl or triisobutyl or aluminum diethyl monochloride with titanium tetrachloride, the present invention being particularly applicable to polyethylene produced in this way and herein after referred to as Ziegler polyethylene. As is Well known, Ziegler polyolefins are solid polymers of substantially linear structures. Such polyolefins, in common with most synthetic polymers, may undergo degradation and discoloration in use (eg as the result of exposure'to light) or in a subsequent processing for example when subjected to milling or other working at elevated temperature, i.e. temperatures above 100 C.

A considerable number of compounds are already known as additives for polymeric compositions based on many of the synthetic polymers now available of other types then polyolefins, which compounds, known as nonstaining antioxidants, impart to such compositions resistance to degradation under the conditions indicated without causing noticeable coloration. In the case of ethylenic polymers produced from the lower olefins by the low pressure process, however, an appreciable number of these known additives have been tested, but it has been found that many of the known additives function in an unexpected manner in that, although they may reduce degradation, they also cause marked color formation. Thus when such additives are present in polymeric materials such as Ziegler polyethylene, there is often pronounced discoloration on working the material at for example 160 C. and sometimes even almost immediately on addition of the additive. However, the phenothiazine derivatives of the present invention, and in particular 10- benzylphenothiazine is effective in arresting degradation and discoloration of such compounds especially low pressure polyethylene at elevated temperatures. Moreover it is particularly effective in preventing degradation of ing illustrative examples:

EXAMPLE I Polymeric materials comprising polyethylene made with a Ziegler catalyst were formed into sheets by milling the polyethylene for various periods of time on a two-roll mill with a milled surface temperature of approximately 160 C. and subsequently pressing the sheeted material in a press which was heated to about 150 C. Various antiom'dants were incorporated in the polyethylene in an amount of 0.1% by weight, and the results are shown in Table I below. In this way lO-benzylphenothiazine was compared with various conventional antioxidants. The color ratings of the samples were determined by a standard reflectivity test and are based on a rating of for a standard white disc. The intrinsic viscosities of the various samples of polyethylene were determined on a 0.1% solution in decalin at C. The I.V. (intrinsic viscosity) of the material after heat rolling provides an indication of the degreeof degradation. The melt index of each sample was also determined.

Table 1 Color Melt Index I.V. Time of milling Time of milling Time of milling Antioxidant 0 30 60 O 30 60 0 30 60 mins. mins. mins. mins. mins. mins. mins. mins. mins.

l0-benzylphenothiazine 84 81 75 .42 0. 48 2. 03 2. 01 2. 14 None 85 78 77 0. 34 0. 28 0.14 2. 25 1.80 18. 4 Oxycresyl camphana-.. 67 58 50 Nonoxyl DCP. 43 45 41 From Table 1 above, it is seen that conventional antioxidants suitered considerable loss in color rating whereas the polyethylene containing IO-benzylphenothiazine suffered little loss in rating and remained substantially as good as the polyethylene with no additive. On the other hand, the polyethylene with no additive suffered a considerable loss of I.V. during only an hour of milling while the polyethylene containing IO-benzylphenothiazine retained its high I.V. EXAMPLE II An oil solution was prepared comprising a solvent refined oil finished with acid and earth treatment and having a high V.l. containing 1.45% by weight of 10- benzylphenothiazine. The solution was left in a clear, stoppered glass tube in full daylight for five weeks and the condition of the oil solution at the end of this period noted. For the purposes of comparison similar oil solutions containing other phenothiazine derivatives were prepared in the same way and exposed to light under the NPA=Nationa1 Petroleum Association color numbers as determined by the ASTM standard method. These results show that phenothiazine and most of its derivatives do not possess good light stability whereas 10-benzylphenothiazine does possess good light stability.

The data in Table II graphically illustrates the superiority of IO-benzylphenothiazine over phenolthiazine and some of its derivatives in regard to color stability. Most noteworthy is the failure of IO-nonylphenothiazine to retain color, because this compound would ordinarily be expected to be somewhat similar to lfi-benzylphenothiazine.

We claim as our invention:

1. A composition consisting essentially of a solid substantially linear polyolefin prepared by polymerization in the presence of a Ziegler type catalyst and between 0.001% and 5% of a phenothiazine having the formula wherein R is a member of the group consisting of a benzyl group, a methylbenzyl group and an ethylbenzyl group.

2. The composition of claim 1, in which the polyolefin is polyethylene.

3. The composition of claim 1, in which the polyolefin is polypropylene.

4. The composition of claim 1, in which R is a benzyl group.

5. The composition of claim 1, in which the phenothiazine is present in an amount of from 0.1% to 0.5% by weight.

References Cited in the file of this patent UNITED STATES PATENTS 2,806,756 Bartram July 2, 1935 2,843,577 Friedlander et a1. July 15, 1958 2,848,444 Brugmann et a1 Aug. 19, 1958 2,868,764 Hirsty Jan. 13, 1959 OTHER REFERENCES Atkins et al.: Development of Additives and Lubricating Oil Composition, 1. and E. Chem., vol. 39, No. April 1947, pages 49l-497.

Murphy at 2.1.: Mode of Action of Phenothiazine Type Antioxidants, Industrial and Engineering Chemistry, vol. 42, pp. 2479-2489, December 1950.

Claims

1. A COMPOSITION CONSISTING ESSENTIALLY OF A SOLID SUBSTANTIALLY LINEAR POLYOLEFIN PREPARED BY POLYMERIZATION IN THE PRESENCE OF A ZIEGLER TYPE CATALYST AND BETWEEN 0.001% AND 5% OF A PHENOTHIAZINE HAVING THE FORMULA